Neudle.com: speech disorder childhood

Differential
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aciduria

acquired immunodeficiency syndrome

acrocyanosis

acute ataxia of childhood

acute cerebellar ataxia

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

advances in neurology

affect, inappropriate

Africa

aggression

agitation

Aicardi-Goutieres syndrome

akinetic mute

alcohol

alcohol intolerance

alcohol, neurologic complications with

alcoholism

alopecia

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alveolar hypoventilation

angiitis, granulomatous of CNS

ankle, swelling of

anomic aphasia

anorexia

antibiotics, neurologic complications with

anxiety

aphasia

aphasia, children

aphasia, classification of

aphasia, recovery from

ataxia telangiectasia

attention deficit disorder with hyperactivity

attention span

atypical

audiologic test to localize site of pathology

audiology

auditory dominance

auditory processing, impaired

autism

autoantibodies

autoimmune disease

autonomic dysfunction

Babinski sign

basal ganglia

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

behavior, combative

behavioral disorder

Benedict's solution test

benign essential tremor

bifid uvula

biotin

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

bone marrow transplantation

brain biopsy, stereotaxic

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

Brown-Vialetto-Van Laere syndrome

bruxism

burning feet

burning feet, differential diagnosis of

CAG repeats

calcification, intracranial

CAT scan, angiography

CAT scan, dense artery sign

catatonia

celiac disease, adult

Central America

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellum, disease of

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral dominance

cerebral embolism

cerebral embolism, mechanical extraction

cerebral palsy

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, young adult

Chagas'disease

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chilbran skin lesions

chromosomal abnormality

chromosome 15

chromosome 7

cirrhosis

cirrhosis, causes of childhood

cleft palate

Clinical Pathologic Conference(C.P.C.)

congenital bilateral perisylvian syndrome

congenital myasthenic syndromes

corpus callosum, infarction of

corpus callosum, lesion of

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying

crying, pathologic

cultured skin fibroblasts

cyanide poison

cytomegalic inclusion disease

cytomegalovirus infection

degenerative diseases of CNS

demyelinating disease

dense basilar artery sign

dense middle cerebral artery sign

dentate nuclei

dentate nuclei, lesion of

depression

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, atonic

diplegia, spastic cerebral

diplopia

disconnection syndrome

doll's head maneuver

dopa responsive dystonia

dysequilibrium syndrome

dyskinesia

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, children

dystonia, laryngeal

dystonia, painful

dystonia, treatment of

dystrophin

DYT1 mutation

echolalia

EDTA(ehtylenediamine tetraacetic acid)

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, sleep

electromyogram

electron microscopy

ELISA

embolism, paradoxical

embolism, vertebral-basilar artery

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, etiology

encephalitis, viral

encephalopathy

encephalopathy, acute

encephalopathy, metabolic

encephalopathy, parainfectious

encephalopathy, progressive

endovascular therapy

enuresis

enzyme, defect

epidemiology of neurology

epilepsia partialis continua

epileptic encephalopathy

epsilon sarcoglycan gene

equinovarus

exome sequencing

eye movement, disorders of

eyedness

face, inexpressive

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial weakness

facial weakness, bilateral

fetal alcohol syndrome

fetus

fever

fine motor function, impaired

finger nose finger test

fingerprint bodies

fish

fluctuate

fluorescene in situ hybridization

folic acid

footedness

frontal lobe, pathologic signs of

fucosidosis

fungal infection, CNS

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallervorden Spatz disease

hallucination

hallucination, visual

head injury, pediatric

hearing problems in children

heavy metal intoxication

hemiparesis, transient

hemiplegia

hemisensory loss

hepatitis

hepatolenticular degeneration(Wilson's disease)

human immunodeficiency virus type 1

hydrocephalus

hydroxyglutaric aciduria

hyperactivity

hyperintense vessel sign

hyperkalemia

hyperosmolality

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hyperreflexia

hypertension

hypertonia

hypokinetic left ventricle

hyponatremia

hypopigmentation of skin

hyporeflexia

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

incoordination

industrial neurologic disorders

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon alpha

intestinal biopsy

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial pressure, increased

Kayser-Fleischer ring

klippel feil syndrome

konzo

lactic acidemia

Landau-Kleffner syndrome

language

language delay

language development, neurologic basis of

language disorders in children

laughing, pathologic

L-dopa

learning disability

learning disability, in children

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

level of consciousness, decreased

liver disease

liver function enzymes

locked-in syndrome

Lyme disease

Lyme disease, children

lymphoma involving CNS

lysosomal storage disease

macrocephaly

macrognathia

magnetic source image

magnetoencephalography

malabsorption syndrome

manganese intoxication

maple syrup urine disease

marche a petits pas

masked facies

medulla oblongata, neoplasm of

medulloblastoma

megalencephaly

megalencephaly, idiopathic

memory, defect of recent

memory, impairment of

meningismus

meningitis

meningitis, aseptic

meningitis, CSF cell count-normal

meningitis, recurrent

meningoencephalitis

mental retardation

mental status, abnormal

MERCI trial

MERS

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

midline defect in children

migraine

mirror writing

misdiagnosis

mitochondrial disease

molecular genetics

monoclonal antibodies

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR, hyperintense vessels

MRI, functional

MRI, negative

MRI, paramagnetic effect

MRI, pelvis

MRI, serial

MRI, T1 weighted high signal foci

MRS

muscle cramp

muscle stiffness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

mutism

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myelinolysis, extrapontine

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nerve biopsy

nerve conduction studies

neurofibromatosis 1

neurologic complications

neurologic complications of, burns

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic examination, focal

neurologic testing

neuromuscular junction

neuronal ceroid-lipofuscinosis

neuropathology

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

non-dominant hemisphere

nonverbal

nystagmus

nystagmus, rotary

nystagmus, spontaneous

opened mouth

operculum syndrome

operculum syndrome, bilateral

osmotic demyelination syndrome

palatal myoclonus

palatopharyngeal incompetence

paralysis, acute areflexic

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paraplegia

paresthesias

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, freezing phenomena in

Parkinsonism syndrome

paroxysmal neurologic deficits

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

polyneuropathy, uremic

pons, infarction of

pons, lesion of

positional head-hanging test

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal

prevention of neurologic disorders

prognathism

prognosis

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis

psychosis, childhood

psychosocial aspects

psychosomatic disease

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriplegia

reading disorder, acquired

recurrent

release phenomena

remote effect of cancer on the nervous system

renal transplantation

renal tubular acidosis

respirations in CNS disease

respirator

restless leg syndrome

reticulum cell sarcoma

reversible neurologic disorder

reversible splenial lesion syndrome

review article

rhabdomyolysis

rheumatic brain disease

rheumatic fever

rheumatic heart disease

riboflavin transporter deficiency

rubella encephalitis, progressive

saccadic eye movements, abnormal

salivation, excessive

seizure, advice to parents and teachers regarding

seizure, children

seizure, focus

seizure, psychosocial aspects of

seizure, recurrent

seizure, surgical treatment of

seizure, treatment of

seizure, workup of

sexual behavior, disorder of

sign language

skin, biopsy

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

speech disorder, childhood

speech disorder, non aphasic

speech lateralization

speech therapy

speech, delayed development of

spinocerebellar ataxia

spinocerebellar ataxia type 7

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

stimulation, deep brain

stimulation, deep brain, bilateral

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

stuttering

stuttering following CVA

subdural hematoma

substantia nigra

suck, poor

symmetric brain lesions

temporal lobe, lesion

temporal lobe, lesion, bilateral

tongue, impaired movements of

tongue, protrusion of

tonic foot response

tonic spasms

torticollis

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, intention

trinucleotide repeats

tuberculosis, miliary

tyrosine hydroxylase deficiency

upgaze, paralysis of

uremia

uremic encephalopathy

uremic twitching

uric acid, low

urine test for metabolic disorders

very long chain fatty acids

vestibulopathy

vibratory sensation, abnormal

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss

visual loss, progressive

visual loss, slow

vitamin supplementation

vitiligo

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

Wada test

walking frame

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weight loss

welder

Wernicke's aphasia

Wernicke's encephalopathy

word-finding difficulty

workup

wrist drop

writing

Showing articles 50 to 100 of 17745 << Previous Next >>

The Syndrome of'Cerebellar'Mutism and Subsequent Dysarthria
Neurol 44:2040-2046, vanDongen,H.R.,et al, 1994

Mental Development of 2-Year-Old Children Exposed to Alcohol in Utero
J Pediatr 120:740-746, Autti-Ramo,I.,et al, 1992

The Landau-Kleffner Syndrome or Acquired Aphasia with Convulsive Disorder
Arch Neurol 49:354-359, 3531992., Paquier,P.F.,et al, 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Acquired Childhood Aphasia
Arch Neurol 47:1324-1328, Loonen,M.C.B.&vanDongen,H.R., 1990

Treatment of Speech and Voice Disorders with Botulinum Toxin
JAMA 264:2671-2675, Ludlow,C.L., 1990

Dyslexia
Editorial, Lancet 2:719-7201989., , 1989

Delayed Speech in Children
BMJ 297:1281-1282, Hall,D., 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Unclear Speech:Recognition & Significance of Unintelligible Speech in Preschool Children
Pediatrics 82:447-452, Coplan,J.&Gleason,J.R., 1988

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Lyme Disease:Acute Focal Meningoencephalitis in a Child
Pediatrics 82:931-934, Feder,H.M.,et al, 1988

Acquired Aphasia in Childhood:Clinical & CT Investigations
Neurol 37:1165-1172, Cranberg,L.D.,et al, 1987

Anatomical Basis for Acquired Fluent Aphasia in Children
Ann Neurol 17:306-309, VanDongen,H.R.,et al, 1985

Recognising & Preventing Duchenne Muscular Dystrophy
BMJ 287:1083-1084, Firth,M.A.,et al, 1983

The Child Who is Slow to Talk
BMJ 285:671-672, Robinson,R.J., 1982

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Acquired Aphasia with Convulsive Disorder:Course & Prognosis
Neurol 30:524-529, Mantovani,J.F.,et al, 1980

Sydenham Chorea:An Update
Neurol 30:331-334, Nausieda,P.A.,et al, 1980

Children's Language Disorders:Recent Research Advances
Ann Neurol 7:497-507, Ludlow,C.L., 1980

Adult Celiac Disease Presenting as Cerebellar Syndrome
Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980

Language Deficits After Apparent Clinical Recovery from Childhood Aphasia
Ann Neurol 6:405-409, Woods,B.,et al, 1979

Aphasias & Related Disturbances
Textbook of Medicine. Ed. R. W. Wilkins Little Brown & Co. , Boston, p. 867, Benson,D.F., 1978

Changing Patterns of Childhood Aphasia
Ann Neurol 3:273, Woods,B.T.,et al, 1978

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

A Fatal Encephalopathy in Chronic Haemodialysis Patients
Lancet 764, Burks,J.S.,et al, 1976

Speech Defects in Children Aged 7 yrs, A National Study
BMJ 253, 1973 Feb., Butler,N.,et al, 1973

Stuttering & Cerebral Ischemia
Letter, NEJM 287:9911972., Rosenfield,D., 1972

Children with Develpmental Language Diorders
Neurol 2:421, Wilson,J.,et al, 1972

Pediatric Neurology
Psych Annals 2:1, , 1972

Learning & Language Disorders in Children
Part II:The School-age Child, Curr Prob Pediatr 1:, 1971 Sept., Gofman,H.,et al, 1971

Learning & Language Disorders in Children
Part I:The School-age Child, Current Problems in Pediatrics 1:1971 Aug., Gofman,H.,et al, 1971

Three Pediatric Problems That Worry Parents
Consultant, MayJun, p. 1270., Bakwin,H.,et al, 1970

Cerebral Dominance & Its Disturbances
Ped Clin North Am 15:759-769, Benson,D.F.,et al, 1968

The Uveomeningoencephalitic Syndrome
Neurol 16, 6031966., Riehl,J.L.,et al, 1966

Non-Aphasia Disorders of Speech
International Jour Neurol 4:207-214, Geschwind,N., 1964

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

Diagnosis and Management of Cerebral Venous Thrombosis:A Scientific Statement From the American Heart Association
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Ocular Myasthenia Gravis, Central Ocular Motor Signs and Unilateral Visual Loss Caused by the Great Neuro-Ophthalmologic Impersonator
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Clinicopathologic Conference, Nutritional Optic Neuropathy Due to Multiple Nutritional Deficits, Including Vitamin A, Copper, and Zinc Deficiencies
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Hyperventilation-Induced Alternating Hemiplegia with Concomitant Hemispheric EEG Slowing in a 7-Year-Old Girl with Headache
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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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Clinicopathologic Conference, Myasthenia Gravis
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Showing articles 50 to 100 of 17745 << Previous Next >>